TY - JOUR
T1 - A General Strategy to Encapsulate Semiconducting Polymers within PEGylated Mesoporous Silica Nanoparticles for Optical Imaging and Drug Delivery
AU - Lu, Feng
AU - Zhan, Chen
AU - Gong, Yi
AU - Tang, Yufu
AU - Xie, Chen
AU - Wang, Qi
AU - Wang, Wenjun
AU - Fan, Quli
AU - Huang, Wei
N1 - Publisher Copyright:
© 2020 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
PY - 2020/6/1
Y1 - 2020/6/1
N2 - Although semiconducting polymers (SPs) have become an important category for optical imaging and phototherapy, their biomedical application is still facing a number of challenges. Herein, a cationic surfactant–assisted approach to encapsulate hydrophobic SPs within highly PEGylated mesoporous silica (mSiO2) nanoparticles with excellent colloidal stability and enhanced fluorescence in aqueous solution is reported. In comparison to the previously reported amphiphilic polymer coating and silification method, this universal strategy not only suppresses the formation of empty polymer micelles and free silica nanoparticles, but also provides high specific surface area for drug loading. As a proof of concept, furan-containing diketopyrrolopyrrole-based semiconducting polymers (PDFT) are coated with mesoporous silica and utilized for fluorescence imaging in the second near-infrared region (NIR-II, 1000–1700 nm) and drug delivery. In vivo blood vessel imaging and tumor imaging are achieved with high resolution (0.21 mm) and signal-to-background ratio (≈4.2). Additionally, pH-responsive drug release and improved therapeutic effect are observed. By choosing desired SPs, different optical imaging and therapeutic modalities can also be achieved, thus the SP@mSiO2 nanostructures obtained here provide numerous opportunities for theranostic applications.
AB - Although semiconducting polymers (SPs) have become an important category for optical imaging and phototherapy, their biomedical application is still facing a number of challenges. Herein, a cationic surfactant–assisted approach to encapsulate hydrophobic SPs within highly PEGylated mesoporous silica (mSiO2) nanoparticles with excellent colloidal stability and enhanced fluorescence in aqueous solution is reported. In comparison to the previously reported amphiphilic polymer coating and silification method, this universal strategy not only suppresses the formation of empty polymer micelles and free silica nanoparticles, but also provides high specific surface area for drug loading. As a proof of concept, furan-containing diketopyrrolopyrrole-based semiconducting polymers (PDFT) are coated with mesoporous silica and utilized for fluorescence imaging in the second near-infrared region (NIR-II, 1000–1700 nm) and drug delivery. In vivo blood vessel imaging and tumor imaging are achieved with high resolution (0.21 mm) and signal-to-background ratio (≈4.2). Additionally, pH-responsive drug release and improved therapeutic effect are observed. By choosing desired SPs, different optical imaging and therapeutic modalities can also be achieved, thus the SP@mSiO2 nanostructures obtained here provide numerous opportunities for theranostic applications.
KW - NIR-II fluorescence imaging
KW - drug delivery
KW - mesoporous silica
KW - optical imaging
KW - semiconducting polymers
UR - http://www.scopus.com/inward/record.url?scp=85085067777&partnerID=8YFLogxK
U2 - 10.1002/ppsc.201900483
DO - 10.1002/ppsc.201900483
M3 - 文章
AN - SCOPUS:85085067777
SN - 0934-0866
VL - 37
JO - Particle and Particle Systems Characterization
JF - Particle and Particle Systems Characterization
IS - 6
M1 - 1900483
ER -